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Osteomyelitis of Maxilla in Infantile Osteopetrosis: A Case Report with Review of Literature

Identifieur interne : 004C24 ( Main/Exploration ); précédent : 004C23; suivant : 004C25

Osteomyelitis of Maxilla in Infantile Osteopetrosis: A Case Report with Review of Literature

Auteurs : Anita Balan [Inde] ; Kl Girija [Inde] ; P. Ranimol [Inde]

Source :

RBID : PMC:5030498

Abstract

Osteopetrosis is a rare genetic disorder that causes generalized sclerosis of bone due to a defect in bone resorption and remodeling. It is usually manifesting in two basic forms: An autosomal dominant benign form (osteopetrosis tarda) and an autosomal recessive malignant form (osteopetrosis congenita). A third form, the intermediate recessive type, has also been reported. Dental abnormality may be attributed to pathological changes in bone remodeling. Osteomyelitis is well documented as a complication of osteopetrosis and is severe and difficult to treat. This is a case of 8-year-old boy with osteopetrosis presenting with the complaint of swelling of left side of face.


Url:
DOI: 10.5005/jp-journals-10005-1095
PubMed: 27672251
PubMed Central: 5030498


Affiliations:


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